Hepatocyte targeting via the asialoglycoprotein receptor

被引:4
作者
Ramirez-Cortes, Fabricio [1 ]
Menova, Petra [1 ]
机构
[1] Univ Chem & Technol, Tech 5, Prague 6, Czech Republic
关键词
PEPTIDE NUCLEIC-ACID; TRANSFER PROTEIN EXPRESSION; ANTISENSE OLIGONUCLEOTIDES; HEPATOCELLULAR-CARCINOMA; CLINICAL-PHARMACOLOGY; BIOLOGICAL EVALUATION; LIGAND-BINDING; LIVER; DELIVERY; SIRNA;
D O I
10.1039/d4md00652f
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review highlights the potential of asialoglycoprotein receptor (ASGPR)-mediated targeting in advancing liver-specific treatments and underscores the ongoing progress in the field. First, we provide a comprehensive examination of the nature of ASGPR ligands, both natural and synthetic. Next, we explore various drug delivery strategies leveraging ASGPR, with a particular emphasis on the delivery of therapeutic nucleic acids such as small interfering RNAs (siRNAs) and antisense oligonucleotides (ASOs). An in-depth analysis of the current status of RNA interference (RNAi) and ASO-based therapeutics is included, detailing approved therapies and those in various stages of clinical development (phases 1 to 3). Afterwards, we give an overview of other ASGPR-targeted conjugates, such as those with peptide nucleic acids or aptamers. Finally, targeted protein degradation of extracellular proteins through ASGPR is briefly discussed.
引用
收藏
页码:525 / 544
页数:20
相关论文
共 200 条
[1]   Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy [J].
Ackermann, Elizabeth J. ;
Guo, Shuling ;
Booten, Sheri ;
Alvarado, Luis ;
Benson, Merrill ;
Hughes, Steve ;
Monia, Brett P. .
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2012, 19 :43-44
[2]   LYTACs that engage the asialoglycoprotein receptor for targeted protein degradation [J].
Ahn, Green ;
Banik, Steven M. ;
Miller, Caitlyn L. ;
Riley, Nicholas M. ;
Cochran, Jennifer R. ;
Bertozzi, Carolyn R. .
NATURE CHEMICAL BIOLOGY, 2021, 17 (09) :937-946
[3]   Disposition characteristics of glycosylated poly(amino acids) as liver cell-specific drug carrier [J].
Akamatsu, K ;
Imai, M ;
Yamasaki, Y ;
Nishikawa, M ;
Takakura, Y ;
Hashida, M .
JOURNAL OF DRUG TARGETING, 1998, 6 (03) :229-239
[4]   SLN124, a GalNAc-siRNA Conjugate Targeting TMPRSS6, Efficiently Prevents Iron Overload in Hereditary Haemochromatosis Type 1 [J].
Altamura, Sandro ;
Schaeper, Ute ;
Dames, Sibylle ;
Loeffler, Kathrin ;
Eisermann, Mona ;
Frauendorf, Christian ;
Muedder, Katja ;
Neves, Joana ;
Muckenthaler, Martina U. .
HEMASPHERE, 2019, 3 (06)
[5]   SLN124, a Galnac-siRNA Conjugate Targeting TMPRSS6, for the Treatment of Iron Overload and Ineffective Erythropoiesis Such As in Beta-Thalassemia [J].
Altamura, Sandro ;
Altamura, Sandro ;
Muckenthaler, Martina U. ;
Dames, Sibylle ;
Frauendorf, Christian ;
Schubert, Steffen ;
Aleku, Manuela ;
Vadolas, Jim ;
Grigoriadis, George ;
Zuegel, Ulrich .
BLOOD, 2018, 132
[6]   Pharmacokinetics and Pharmacodynamics of GalNAc-Conjugated siRNAs [J].
An, Guohua .
JOURNAL OF CLINICAL PHARMACOLOGY, 2024, 64 (01) :45-57
[7]  
Armandi A., 2022, OBESITY DIABETES, DOI [10.1007/1642021561, DOI 10.1007/1642021561]
[8]   CARBOHYDRATE-SPECIFIC RECEPTORS OF THE LIVER [J].
ASHWELL, G ;
HARFORD, J .
ANNUAL REVIEW OF BIOCHEMISTRY, 1982, 51 :531-554
[9]  
Ashwell G., 1974, ADV ENZYMOL RELAT AR, DOI [10.1002/9780470122860.ch3, DOI 10.1002/9780470122860.CH3]
[10]   Mechanistic Pharmacokinetics and Pharmacodynamics of GalNAc-siRNA: Translational Model Involving Competitive Receptor-Mediated Disposition and RISC-Dependent Gene Silencing Applied to Givosiran [J].
Ayyar, Vivaswath S. ;
Song, Dawei .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2024, 113 (01) :176-190